Evidence map›Paper›PMID 23149012›Full record

ArticleBiomaterials2013

Understanding the host response to cell-laden poly(ethylene glycol)-based hydrogels.

Mark D Swartzlander, Aaron D Lynn, Anna K Blakney, Themis R Kyriakides, Stephanie J Bryant

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.7field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 33 citations in OpenAlex.

  1. Modeling Uterine Fibroids Using Bioengineered Hydrogels.ACS biomaterials science & engineering · 2025
    Article
  2. Article
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  4. Intravital three-dimensional bioprinting.Nature biomedical engineering · 2020
    Article
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  10. Drug discovery today. Disease models · 2017
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Mark D SwartzlanderDepartment of Chemical & Biological Engineering, University of Colorado, Boulder, CO 80303, USA. Mark.Swartzlander@colorado.edu
Aaron D Lynn
Anna K Blakney
Themis R Kyriakides
Stephanie J Bryant
University of Colorado Boulder · USYale University · US

Funding

MCP-1 and attenuation of the foreign body responseR01GM072194 · NIGMS · YALE UNIVERSITY · PI KYRIAKIDES, THEMIS R · 2005 to 2018
$4.7M
Modulating the Host Response to Tissue Engineering ScaffoldsR03DE019505 · NIDCR · UNIVERSITY OF COLORADO · PI BRYANT, STEPHANIE J · 2010 to 2011
$231k
Howard Hughes Medical InstituteNIDCR NIH HHS 1R03DE019505NIDCR NIH HHS R03 DE019505NIGMS NIH HHS R01 GM072194
6 · The paper itself

Abstract

Poly(ethylene glycol) (PEG)-based hydrogels are promising in situ cell carriers for tissue engineering. However, their success in vivo will in part depend upon the foreign body reaction (FBR). This study tests the hypothesis that the FBR affects cells encapsulated within PEG hydrogels, and in turn influences the severity of the FBR. Fibroblasts were encapsulated within PEG hydrogels containing RGD to support cell attachment. Macrophages were seeded on top of cell-laden hydrogels to mimic in vivo macrophage interrogation and treated with lipopolysaccharide to induce an inflammatory phenotype. The presence of activated macrophages reduced fibroblast gene expression for extracellular matrix molecules and remodeling, but stimulated VEGF and IL-1β gene expression. Fibroblasts impacted macrophage phenotype leading to increased iNOS, IL-1β and TNF-α expressions. Syngeneic cell-laden and acellular hydrogels were also implanted subcutaneously into C57bl/6 mice for 2, 7 and 28 days. Encapsulated fibroblasts secreted collagen type I during the first week, but tissue deposition and cellularity decreased by 28 days. The presence of encapsulated fibroblasts led to greater acute inflammation, but did not influence the fibrotic response. In summary, this work emphasizes the importance of the host response in tissue engineering, and the potentially deleterious impact it may have on cell-laden synthetic scaffolds.

Indexed as

AnimalsBiocompatible MaterialsCell LineHydrogelsImmunity, InnateMacrophage ActivationMacrophagesMaterials TestingMiceNIH 3T3 CellsPolyethylene GlycolsBiocompatible MaterialsHydrogelsPolyethylene Glycols

Identifiers

PMID23149012
PMCPMC3683297
OpenAlexW2132306201

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.